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K Cowell

Showing results (61-70 of 266) with videos related to

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British Journal of Cancer|June 1, 1993
Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 geneJ K Cowell, N Groves, P Baird
Genes, Chromosomes & Cancer|February 25, 2017
Promotion of invasion by mutant RAS is dependent on activation of the WASF3 metastasis promoter geneYong Teng, Lambert Ngoka, John K Cowell
Blood|June 10, 2009
Genetic fingerprinting of the development and progression of T-cell lymphoma in a murine model of atypical myeloproliferative disorder initiated by the ZNF198-fibroblast growth factor receptor-1 chimeric tyrosine kinaseMingqiang Ren, Xiurong Li, John K Cowell
BMC Neuroscience|May 17, 2011
The temporal and spatial expression pattern of the LGI1 epilepsy predisposition gene during mouse embryonic cranial developmentJeane Silva, Guanghu Wang, John K Cowell
Oncogene|January 18, 1996
A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 geneJ K Cowell, B Bia, A Akoulitchev
The Journal of Biological Chemistry|July 12, 2007
c-Abl-mediated phosphorylation of WAVE3 is required for lamellipodia formation and cell migrationKhalid Sossey-Alaoui, Xiurong Li, John K Cowell
Oncogene|February 20, 2004
CLCA2 tumour suppressor gene in 1p31 is epigenetically regulated in breast cancerXiurong Li, John K Cowell, Khalid Sossey-Alaoui
Genomics|January 25, 2000
Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase proteinI H Still, P Vince, J K Cowell
International Journal of Molecular Medicine|December 16, 1998
Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisationR G Grundy, R Aledo, J K Cowell
International Journal of Molecular Medicine|April 14, 2000
A new region of synteny between human chromosome 1p22 and mouse chromosome 5D M Chelsea, T Roberts, J K Cowell
Pageof 27

Showing results (61-70 of 266) with videos related to

Sort By:
Pageof 27
British Journal of Cancer|June 1, 1993
Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 geneJ K Cowell, N Groves, P Baird
Genes, Chromosomes & Cancer|February 25, 2017
Promotion of invasion by mutant RAS is dependent on activation of the WASF3 metastasis promoter geneYong Teng, Lambert Ngoka, John K Cowell
Blood|June 10, 2009
Genetic fingerprinting of the development and progression of T-cell lymphoma in a murine model of atypical myeloproliferative disorder initiated by the ZNF198-fibroblast growth factor receptor-1 chimeric tyrosine kinaseMingqiang Ren, Xiurong Li, John K Cowell
BMC Neuroscience|May 17, 2011
The temporal and spatial expression pattern of the LGI1 epilepsy predisposition gene during mouse embryonic cranial developmentJeane Silva, Guanghu Wang, John K Cowell
Oncogene|January 18, 1996
A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 geneJ K Cowell, B Bia, A Akoulitchev
The Journal of Biological Chemistry|July 12, 2007
c-Abl-mediated phosphorylation of WAVE3 is required for lamellipodia formation and cell migrationKhalid Sossey-Alaoui, Xiurong Li, John K Cowell
Oncogene|February 20, 2004
CLCA2 tumour suppressor gene in 1p31 is epigenetically regulated in breast cancerXiurong Li, John K Cowell, Khalid Sossey-Alaoui
Genomics|January 25, 2000
Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase proteinI H Still, P Vince, J K Cowell
International Journal of Molecular Medicine|December 16, 1998
Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisationR G Grundy, R Aledo, J K Cowell
International Journal of Molecular Medicine|April 14, 2000
A new region of synteny between human chromosome 1p22 and mouse chromosome 5D M Chelsea, T Roberts, J K Cowell
Pageof 27